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. 2021 Nov 25;11(12):2196. doi: 10.3390/diagnostics11122196

Table 1.

Mutational analysis in the pretreatment tissue samples and in plasma ctDNA at disease progression.

Patients Characteristics Tissue Molecular Analysis (Baseline) Plasma Molecular Analysis (PD)
Pt.# Age Gender Smoking Status ALK ROS PD-L1 KRAS Other KRAS
(Idylla)
KRAS
(NGS)
Other
1 71 M 2 0 0 1 wt DDR2 G12C+ G12C+ MAP2K1
2 56 M 1 0 0 0 G12C− CTNNB1 wt wt BRAFV600E
3 65 M 2 0 0 0 wt None wt wt none
4 73 M 2 0 0 0 wt None G12C+ G12C+ PI3K
5 65 M 1 0 0 1 wt P53 wt wt none
6 64 F 1 0 0 1 wt P53 G12V G12V none
7 70 M 1 0 0 0 wt P53 G12C+ G12C+ MAP2K1
8 77 F 2 0 0 1 G12C− P53 wt wt P53
9 76 M 2 0 0 0 G12F p53 wt wt none
10 66 M 1 0 0 1 wt p53; STK11 G12C+ G12C+ EGFR
11 65 M 1 0 0 1 wt P53 wt wt none
12 64 F 1 0 0 1 wt P53 wt wt none
13 72 M 2 0 0 0 wt p53; MET wt wt EGFR
14 58 F 2 0 0 1 Q61H none wt wt none
15 72 F 2 0 0 1 wt none wt wt none
16 67 F 2 0 0 1 Q61K none wt wt none
17 77 F 2 0 0 0 wt AKT wt wt EGFR del 19
18 84 M 1 0 0 0 G12D STK11 G12D G12D none
19 71 M 1 0 0 1 wt STK11; CTNNB1 wt wt
20 44 M 2 0 0 0 wt none wt wt none
21 81 M 2 0 0 1 G12F p53; NRAS; ERBB4 G12C+ G12C+ P53
22 63 F 2 0 0 2 wt P53 wt wt PIK3A
23 56 M 2 0 0 2 wt P53 G12C+ G12C+ P53
24 76 M 2 0 0 2 G12C− none wt wt BRAF V600
25 78 M 1 0 0 2 G12D none G12D G12D BRAF V600E
26 65 F 1 0 0 2 G12D P53 G12D G12D P53
27 60 M 1 0 0 2 wt none G12C+ G12C+ BRAFV600
28 65 F 0 0 0 2 wt none G12C+ G12C+ G12D
29 55 M 2 0 0 2 wt none wt wt MET
30 62 F 1 0 0 2 G12C− none wt wt PIK3A
31 69 M 2 0 0 2 G12C− none wt wt MAP2K1
32 58 M 2 0 0 2 G12C− none wt wt BRAFv600E
33 71 F 0 0 0 0 wt EGFR; MET wt wt T790M
34 60 M 0 0 0 2 wt EGFR; p53 wt wt T790M
35 64 M 2 1 0 0 wt p53; PIK3A wt wt none
36 78 M 0 0 0 0 wt EGFR; PIK3A wt wt T790M
37 87 M 2 1 0 2 wt none G12C+ G12C+ EGFR
38 35 M 0 0 0 1 wt EGFR wt wt none

G12C−: patients with the baseline tissue samples positive for the KRAS G12C mutation who became negative in ctDNA at PD. G12C+: patients with the baseline tissue samples negative for the KRAS G12C mutation who acquired a mutation in ctDNA at PD. PD: progressive disease.